http://identifiers.org/hco/11/GRCh38#103907202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6379254-C-A

103907202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 3 prime UTR variant
orthologous variants: 6379254-C-T

103907331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 3 prime UTR variant
orthologous variants: 6379125-C-T

http://identifiers.org/hco/11/GRCh38#103907376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6379083-C-A

103907418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 3 prime UTR variant
orthologous variants: 6379043-A-G

103907471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 3 prime UTR variant
orthologous variants: 6378983-G-T

http://identifiers.org/hco/11/GRCh38#103907514-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6378940-A-C

103907552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 3 prime UTR variant
orthologous variants: 6378902-G-A

103907577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 3 prime UTR variant
orthologous variants: 6378877-A-G

103907594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 3 prime UTR variant
orthologous variants: 6378860-T-C

103907666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 3 prime UTR variant
orthologous variants: 6378808-C-T

103907682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 3 prime UTR variant
orthologous variants: 6378792-A-G

103907933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 3 prime UTR variant
orthologous variants: 6378579-G-T

103907939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 3 prime UTR variant
orthologous variants: 6378573-A-G

http://identifiers.org/hco/11/GRCh38#103907953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6378560-C-A

103907953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 3 prime UTR variant
orthologous variants: 6378560-C-T

103907962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 3 prime UTR variant
orthologous variants: 6378551-T-C

103908038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 3 prime UTR variant
orthologous variants: 6378503-A-G

103908038-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 3 prime UTR variant
orthologous variants: 6378503-A-T

103908048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 3 prime UTR variant
orthologous variants: 6378493-A-G

http://identifiers.org/hco/11/GRCh38#103908086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6378457-C-A

103908354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 3 prime UTR variant
orthologous variants: 6378182-T-C

http://identifiers.org/hco/11/GRCh38#103908371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6378172-C-A

103908371-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 3 prime UTR variant
orthologous variants: 6378172-C-G

103908371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 3 prime UTR variant
orthologous variants: 6378172-C-T

103908593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 3 prime UTR variant
orthologous variants: 6378069-T-C

http://identifiers.org/hco/11/GRCh38#103908796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6377875-C-A

103908796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 3 prime UTR variant
orthologous variants: 6377875-C-T

103908960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 3 prime UTR variant
orthologous variants: 6377698-G-A

103909067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 3 prime UTR variant
orthologous variants: 6377579-G-T

http://identifiers.org/hco/11/GRCh38#103909172-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6377479-A-C

103909175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 3 prime UTR variant
orthologous variants: 6377474-T-C

103909184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 3 prime UTR variant
orthologous variants: 6377465-G-T

103909215-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 3 prime UTR variant
orthologous variants: 6377438-G-C

103909215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 3 prime UTR variant
orthologous variants: 6377438-G-T

103909234-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 3 prime UTR variant
orthologous variants: 6377419-G-C

103909234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 3 prime UTR variant
orthologous variants: 6377419-G-T

103909429-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 3 prime UTR variant
orthologous variants: 6377241-A-T

103909574-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 3 prime UTR variant
orthologous variants: 6377107-T-G

103909590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 3 prime UTR variant
orthologous variants: 6377092-C-T

103909687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 3 prime UTR variant
orthologous variants: 6377025-C-T

103909838-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6376867-C-G

103909838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6376867-C-T

103909881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6376825-C-T

103909885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6376821-C-T

103909936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6376769-G-A

103909936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6376769-G-T

103909997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6376719-T-C

103910022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6376691-A-G

103910024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6376689-T-C

103918018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6376201-T-C

103918282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6375480-G-A

103918474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6375319-T-C

103918474-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6375319-T-G

103918551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6375247-A-G

103918811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6374985-G-A

103918826-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6374970-A-T

103919146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6374636-C-T

103919182-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6374603-G-C

103919190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6374595-A-G

103919460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6374315-T-C

103920193-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6373918-T-G

103920227-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6373885-T-G

103920432-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6373716-T-A

103920525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6373651-G-A

103920525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6373651-G-T

103920611-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6373562-T-G

103920613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6373559-G-T

103920676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6373496-A-G

103920687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6373485-C-T

103920785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6373386-G-A

103920791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6373379-T-C

103920831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6373230-G-T

103920904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6373161-C-T

103921108-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6372989-T-G

103921164-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6372931-G-C

http://identifiers.org/hco/11/GRCh38#103923652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6364390-C-A

103923652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6364390-C-T

103923653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6364389-C-T

103923973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6364131-A-G

103924034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6364074-G-A

103924367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6363834-C-T

103926307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6361812-G-A

103926501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6361601-G-A

103926501-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6361601-G-C

103927075-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: missense variant
orthologous variants: 6359752-C-G

103927241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6359616-T-C

103927672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6352159-G-T

103927859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6352353-T-C

103928099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6352602-A-G

103928386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6353136-G-A

103928444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6353192-G-A

103928444-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6353192-G-C

http://identifiers.org/hco/11/GRCh38#103928558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6353308-C-A

103929096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6353934-G-A

103929333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron_variant, undefined
orthologous variants: 6354114-T-C

http://identifiers.org/hco/11/GRCh38#103929351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#6348428-C-A

103929351-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron_variant, undefined
orthologous variants: 6348428-C-G

103929351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron_variant, undefined
orthologous variants: 6348428-C-T

103929470-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron_variant, undefined
orthologous variants: 6348317-A-T

103929828-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6348022-C-G

103930060-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6347842-T-A

http://identifiers.org/hco/11/GRCh38#103930134-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6347767-A-C

103930360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6347543-C-T

103932662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6347184-G-A

103932698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6347148-T-C

103932805-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6347015-G-C

103932805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6347015-G-T

103933186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6346736-G-A

103933186-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6346736-G-C

103933272-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6346649-T-A

103933348-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6346572-A-T

103933507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6346432-G-A

103933507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6346432-G-T

http://identifiers.org/hco/11/GRCh38#103933516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6346423-C-A

103933630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6346310-C-T

103933715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6346238-C-T

103933788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6346163-G-A

103933954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6346011-T-C

http://identifiers.org/hco/11/GRCh38#103934140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6345769-C-A

103934206-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6345702-C-G

103934248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6345657-C-T

http://identifiers.org/hco/11/GRCh38#103934250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6345655-C-A

103934426-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6345531-C-G

103934922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6345432-C-T

103935489-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6345318-A-T

103935700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6345132-T-C

103935714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6345120-T-C

103935766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6345070-T-C

103935795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6345033-T-C

103935795-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6345033-T-G

103935846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6344980-G-A

103936671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6343909-T-C

103937111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6343436-C-T

103937166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6343377-A-G

103937192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6343350-T-C

http://identifiers.org/hco/11/GRCh38#103937339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6343018-C-A

103937339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6343018-C-T

103937368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6342983-G-A

103939650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6342745-T-C

103939690-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6342705-T-A

103939722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6342693-T-C

103939764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6342654-G-A

103939764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6342654-G-T

103939998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6342428-A-G

103940129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6342351-G-T

103940142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6342336-A-G

103940220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6341619-T-C

103940234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6341605-G-A

103940339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6341509-C-T

103940506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6341170-T-C

103940639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6341054-G-T

103941006-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6340664-T-A

103941118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6340556-G-A

103941135-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6340546-T-G

103941268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6340417-G-A

103941374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6340352-T-C

103941466-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6340294-T-G

103941521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6340238-C-T

103941551-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6340208-C-G

103941551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6340208-C-T

103941654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6340107-G-T

103941750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6340056-A-G

103941783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6340021-G-A

103941801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6340003-G-A

103941808-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6339996-T-G

103941919-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6339899-A-T

103941997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6339828-T-C

103942042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6339793-T-C

103942577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6339055-G-A

103942631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6338998-A-G

http://identifiers.org/hco/11/GRCh38#103943435-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6337456-A-C

103943435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6337456-A-G

103943571-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: missense variant
orthologous variants: 6337320-T-G

http://identifiers.org/hco/11/GRCh38#103943670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6337221-C-A

103943670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6337221-C-T

103943730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6337161-G-T

http://identifiers.org/hco/11/GRCh38#103943731-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6337160-A-C

http://identifiers.org/hco/11/GRCh38#103943737-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6337154-A-C

http://identifiers.org/hco/11/GRCh38#103943739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6337152-C-A

103943739-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6337152-C-G

http://identifiers.org/hco/11/GRCh38#103943765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6337129-C-A

103943765-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6337129-C-G

103943765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6337129-C-T

103943929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6336980-G-A

103944085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6336832-C-T

103944108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6336810-T-C

103944118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6336800-T-C

103944139-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6336788-T-G

103944197-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6336730-A-T

103944222-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6336705-C-G

103944610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6336277-A-G

103946330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron_variant, undefined
orthologous variants: 6335036-G-T

103946343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron_variant, undefined
orthologous variants: 6335023-G-A

103946364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron_variant, undefined
orthologous variants: 6335011-G-T

103946429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron_variant, undefined
orthologous variants: 6334943-G-T

http://identifiers.org/hco/11/GRCh38#103946549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6334826-C-A

103946942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6333905-C-T

103947026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6333822-T-C

103947171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6333674-T-C

103947575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6333471-T-C

103947582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6333464-T-C

103947618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6333428-T-C

103947618-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6333428-T-G

103947632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6333414-T-C

103947637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6333409-G-T

103947708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: missense variant
orthologous variants: 6333338-G-A

http://identifiers.org/hco/11/GRCh38#103947742-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6333304-A-C

http://identifiers.org/hco/11/GRCh38#103947874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6333176-C-A

103947913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6333137-A-G

103948230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6332803-T-C

103948662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6332363-C-T

103948678-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6332347-G-C

http://identifiers.org/hco/11/GRCh38#103950985-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6330184-A-C

103950991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6330178-C-T

103951038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6330130-G-T

103951234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6329943-A-G

103951668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6329547-T-C

103951682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6329533-C-T

103951683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6329532-T-C

103952434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6328884-T-C

103952600-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6328690-T-A

103953002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6328368-G-A

103953002-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6328368-G-C

103953187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6327830-G-A

103953209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6327805-T-C

103953248-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6327757-A-T

103953446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6327570-T-C

103953469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6327553-T-C

103953984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6326863-A-G

103954233-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6326642-T-G

103954264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6326610-A-G

103954584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6326323-A-G

103954788-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6326125-C-G

http://identifiers.org/hco/11/GRCh38#103955209-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6326085-A-C

http://identifiers.org/hco/11/GRCh38#103955233-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#6326061-A-C

103955233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron_variant, undefined
orthologous variants: 6326061-A-G

103955260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6326035-G-A

103955353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6325944-G-A

103955443-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6325852-C-G

103955463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6325840-G-T

103955532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6325786-C-T

103957793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6325290-G-A

103958084-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6321435-A-T

103958190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6321332-G-A

103958239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6321267-A-G

103958253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6321253-G-A

103958335-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6321183-T-A

103958347-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6321171-G-C

http://identifiers.org/hco/11/GRCh38#103958457-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6321066-A-C

103958803-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6320600-A-T

103958810-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6320593-A-T

103961809-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6320028-C-G

103961809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6320028-C-T

103961811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6320026-G-A

103961815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6320019-A-G

103961889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6319952-C-T

103961989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6319788-G-A

103961995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6319782-T-C

103962044-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6319732-T-A

103962091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6319695-T-C

103962150-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6319633-A-T

103962291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6319498-T-C

103962484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6319303-C-T

103962495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6319292-T-C

http://identifiers.org/hco/11/GRCh38#103962546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6319244-C-A

http://identifiers.org/hco/11/GRCh38#103962677-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6319144-A-C

103962681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6319140-G-A

103962852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6318999-T-C

103962896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6318966-T-C

103962944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6318913-T-C

103963139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6318740-G-A

103963140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6318739-T-C

103963316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6318566-A-G

http://identifiers.org/hco/11/GRCh38#103963544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6318377-C-A

103963544-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6318377-C-G

103963694-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6318253-C-G

103963847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6318100-C-T

103964215-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6316629-A-T

103964222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6316622-T-C

103964480-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6316450-T-A

103964480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6316450-T-C

103965161-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6315799-T-G

103965167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6315793-C-T

103965193-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6315765-G-C

103965691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6315318-T-C

103965871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6315145-A-G

103965966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6315051-C-T

103966697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6314212-G-A

103966700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6314205-A-G

103966700-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6314205-A-T

103966983-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6313967-G-C

103967041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6313928-C-T

103978357-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6309432-T-G

103978462-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6309357-A-T

103978837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6308987-T-C

103978853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6308966-C-T

103978938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6308891-T-C

103979440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6305386-C-T

103979540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6305287-G-A

http://identifiers.org/hco/11/GRCh38#103980128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6304325-C-A

103980264-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6304192-T-G

103980294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6304162-G-A

103980297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6304159-T-C

103980652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6303803-C-T

103980699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6303748-C-T

103980870-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6303588-C-G

103980926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6303525-C-T

103980965-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6303504-T-A

103981011-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6303477-C-G

103981011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6303477-C-T

103981596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6303336-T-C

103981745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6303135-C-T

103982029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6302886-C-T

103982032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6302883-C-T

103988096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6302588-C-T

http://identifiers.org/hco/11/GRCh38#103988109-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6302575-A-C

103988231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6302451-G-T

103988330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6302349-T-C

http://identifiers.org/hco/11/GRCh38#103988489-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6302186-A-C

103989204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6301444-A-G

103989205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6301443-T-C

103989219-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6301429-A-T

103989231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6301417-C-T

103989376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6301299-G-A

103991203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6299872-A-G

103991297-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6299783-C-G

103991783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6299109-G-A

103991858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6299039-G-A

103991885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6299021-C-T

103992112-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6298847-C-G

103992226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6298740-T-C

103992286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6298689-T-C

103992411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6298203-T-C

103992552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6298087-G-A

103992644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6298009-G-A

103992703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6297943-A-G

103992742-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6297904-G-C

http://identifiers.org/hco/11/GRCh38#103992824-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6297824-A-C

103993591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6297400-T-C

http://identifiers.org/hco/11/GRCh38#103993666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6297321-C-A

103993739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6297244-C-T

103993760-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6297223-G-C

103993787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6297202-G-A

103993794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6297195-T-C

103993958-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6297055-T-A

103993964-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6297049-T-A

103993964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6297049-T-C

http://identifiers.org/hco/11/GRCh38#103994015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6297003-C-A

103994015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6297003-C-T

103994236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6295085-T-C

103994300-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6295018-T-A

103994558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6294799-A-G

103994640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6294719-A-G

103994680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6294684-A-G

103995549-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6294448-C-G

103995553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6294444-T-C

103995574-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6294423-G-C

103995577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6294420-C-T

103995633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6294364-T-C

103995884-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6294094-T-G

103995956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6294021-G-A

103995956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6294021-G-T

103995996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6293985-T-C

103996174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: missense variant
orthologous variants: 6293826-T-C

103996269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6293733-A-G

103996269-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6293733-A-T

103996310-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6293705-C-G

103996384-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6293633-T-G

103996603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6293420-A-G

103996698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6293330-A-G

103996927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6293147-T-C

103996937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6293137-C-T

103997141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6292948-G-A

103997490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6292605-T-C

103997538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6292558-T-C

103998285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6291957-G-A

103998425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6291822-G-A

103998636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6291634-T-C

http://identifiers.org/hco/11/GRCh38#103998707-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6291568-A-C

103999012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6289949-C-T

103999105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6289866-T-C

103999209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6289755-G-A

103999296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6289686-T-C

103999359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6289619-A-G

103999914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6288953-A-G

103999914-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6288953-A-T

103999927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6288940-A-G

http://identifiers.org/hco/11/GRCh38#103999937-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6288778-A-C

103999937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6288778-A-G

104000111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: missense variant
orthologous variants: 6288614-C-T

104000845-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6287908-T-A

104000845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6287908-T-C

104000982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6287779-G-A

104001040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6287720-G-A

http://identifiers.org/hco/11/GRCh38#104001145-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6287628-A-C

104001460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6287393-G-A

http://identifiers.org/hco/11/GRCh38#104001668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6287201-C-A

104001745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6287129-A-G

104001803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6287076-T-C

104001840-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6287040-G-C

104002718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6286633-C-T

104002805-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6286560-T-G

104002822-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6286543-A-T

http://identifiers.org/hco/11/GRCh38#104002893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6286473-C-A

http://identifiers.org/hco/11/GRCh38#104005328-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6284865-A-C

104005329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6284864-G-A

104005329-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6284864-G-C

104005475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6284706-A-G

104005593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron_variant, undefined
orthologous variants: 6284592-T-C

104005611-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6284574-T-A

104005659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6284520-T-C

104005705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6284476-G-A

104005747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6284434-A-G

104005796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6284392-A-G

104005887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6284323-G-A

104005890-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6284320-T-G

104005949-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6284259-C-G

104005949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6284259-C-T

104007212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6283818-A-G

http://identifiers.org/hco/11/GRCh38#104007522-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6283515-A-C

104007522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6283515-A-G

104007546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6283489-A-G

104007613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6283419-G-A

104007624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6283408-A-G

104007896-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6283103-T-A

104018042-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6281005-T-A

104018308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6280791-G-A

104018311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6280788-C-T

104018392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6280665-T-C

http://identifiers.org/hco/11/GRCh38#104018412-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6280608-A-C

104019024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6279838-T-C

104019024-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6279838-T-G

104019329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6279582-A-G

http://identifiers.org/hco/11/GRCh38#104019346-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6279565-A-C

104019446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6279502-A-G

104019545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6279418-C-T

104019546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6279417-G-A

104019546-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6279417-G-C

104020096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6278943-T-C

104020261-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6278798-G-C

104021496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6277528-T-C

104021751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6277270-T-C

104021773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6277248-G-T

104022296-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6276742-A-T

104022385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6276654-G-A

104022530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6276517-G-A

104022590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6276456-A-G

104022668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6276378-T-C

104022692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6276368-A-G

104022885-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6276271-T-A

104022885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6276271-T-C

104022906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6276249-A-G

104022980-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6276171-A-T

104022998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6276153-A-G

104023032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6276111-C-T

104023104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6276032-T-C

104023127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6276009-A-G

104023127-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6276009-A-T

104024008-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6275201-C-G

http://identifiers.org/hco/11/GRCh38#104024021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6275194-C-A

104024046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6275148-C-T

104024077-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6275117-A-T

104024097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6275098-G-A

104024097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6275098-G-T

104025045-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6274473-T-G

http://identifiers.org/hco/11/GRCh38#104025476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6273991-C-A

104025476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6273991-C-T

104025716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6273857-A-G

104025767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6273807-A-G

http://identifiers.org/hco/11/GRCh38#104025829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6273745-C-A

104025934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6273641-T-C

104029685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6272480-C-T

104029704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6272462-G-T

104029733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6272444-T-C

104029842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6272342-A-G

104029913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6272255-A-G

104032303-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6270481-G-C

104032303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6270481-G-T

104032654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6269744-T-C

http://identifiers.org/hco/11/GRCh38#104032928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6269208-C-A

104033156-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6269038-G-C

104033339-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron_variant, undefined
orthologous variants: 6268858-T-A

104033390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6268806-G-A

104033571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6268646-T-C

104033881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6268253-C-T

104033956-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6268166-T-A

104034332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6267719-T-C

104035576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6266994-T-C

http://identifiers.org/hco/11/GRCh38#104036476-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6266676-A-C

104036476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6266676-A-G

104036486-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6266666-A-T

http://identifiers.org/hco/11/GRCh38#104036487-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6266665-A-C

104036688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 6266489-T-C

http://identifiers.org/hco/11/GRCh38#104036759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6266430-C-A

104036759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 6266430-C-T

104037159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron_variant, missense_variant
orthologous variants: 6266011-G-A

104037223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron_variant, missense_variant
orthologous variants: 6265947-T-C

104037525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron_variant, missense_variant
orthologous variants: 6265645-C-T

104037744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron_variant, stop_gained
orthologous variants: 6265426-C-T

104037768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron_variant, missense_variant
orthologous variants: 6265402-T-C

104038239-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 6264905-T-A

104038317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 6264844-G-T

http://identifiers.org/hco/11/GRCh38#104038335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6264825-C-A

http://identifiers.org/hco/11/GRCh38#104038340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6264820-C-A

http://identifiers.org/hco/11/GRCh38#104038430-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6264720-A-C

104038430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 6264720-A-G

http://identifiers.org/hco/11/GRCh38#104038431-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6264719-A-C

104038431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 6264719-A-G

104038489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 6264149-G-A

104038489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 6264149-G-T

104038503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 6264132-A-G

104038508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 6264127-A-G

104038556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 6264079-G-T

104038587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 6264048-T-C

104038587-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 6264048-T-G

http://identifiers.org/hco/11/GRCh38#104038630-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6264014-C-A

104038641-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 6264003-T-G

http://identifiers.org/hco/11/GRCh38#104038694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6263977-C-A

104038694-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 6263977-C-G

http://identifiers.org/hco/11/GRCh38#104038703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6263968-C-A

104038703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 6263968-C-T

104038816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 6263866-G-T

104039109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 6263685-C-T

104039421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6263232-C-T

http://identifiers.org/hco/11/GRCh38#104039663-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6263038-A-C

104039715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6262977-G-T

104039834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6262682-A-G

104039891-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6262614-T-A

104040485-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6262053-C-G

104040485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6262053-C-T

104040570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6261996-G-T

104040601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6261962-C-T

104042344-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6257062-T-G

104042865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6256132-T-C

104043170-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6255860-A-T

104043226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6255813-T-C

104043227-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6255812-C-G

104045398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6254950-C-T

104045701-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6254674-T-A

104045825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6254564-G-A

104045850-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6254539-A-T

104045872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6254519-A-G

104045993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6254425-G-T

http://identifiers.org/hco/11/GRCh38#104046016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6254402-C-A

104048015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6253320-A-G

104048369-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6253031-T-G

104048372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6253028-C-T

104048703-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6252715-G-C

104048720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6252708-C-T

http://identifiers.org/hco/11/GRCh38#104048775-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6252658-A-C

104053713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6252227-C-T

104053760-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6252170-T-A

http://identifiers.org/hco/11/GRCh38#104054200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6251784-C-A

104054200-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6251784-C-G

104054200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6251784-C-T

104054292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6251709-C-T

104054723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6251213-G-A

104054723-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6251213-G-C

104054810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6251126-G-A

http://identifiers.org/hco/11/GRCh38#104054866-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6251058-A-C

104055207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6250561-C-T

104059320-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6250093-T-A

104059320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6250093-T-C

http://identifiers.org/hco/11/GRCh38#104059426-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6249991-A-C

104059426-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6249991-A-T

104059438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6249979-C-T

http://identifiers.org/hco/11/GRCh38#104059675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6249764-C-A

104059675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6249764-C-T

104059835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6249594-A-G

104060446-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6249034-A-T

104060451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6249027-T-C

104060492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6248986-G-A

104060492-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6248986-G-C

104079922-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: -T-G

104079926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: -T-C

104080094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: -T-C

104080094-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: -T-G

104081134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6244920-C-T

http://identifiers.org/hco/11/GRCh38#104081415-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6244638-A-C

104081415-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6244638-A-T

104081689-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6244351-T-G

104082392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6242638-G-T

104090095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6240703-A-G

104090114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6240682-G-A

104090114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6240682-G-T

104090119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6240677-G-T

http://identifiers.org/hco/11/GRCh38#104090610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6240329-C-A

104090612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6240327-G-A

104090702-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6240251-A-T

104091131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6239875-C-T

104091218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6239797-A-G

104091415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6239610-T-C

104091546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6239480-G-A

104091546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6239480-G-T

104091560-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6239468-C-G

104091574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6239454-C-T

104091698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6239365-G-A

104091769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6239296-G-A

104091859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6239206-T-C

104092369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6238437-A-G

104092600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6237607-A-G

104092942-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6237289-G-C

104093072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6237181-C-T

104093112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6237141-G-A

104093112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6237141-G-T

104093113-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6237140-C-G

104094780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6231994-C-T

104094944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6231817-C-T

104094957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6231804-A-G

104095038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6231635-C-T

104095095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6231534-A-G

104095115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6231514-T-C

104095182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6231447-C-T

104095285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6231379-G-A

104095426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6231251-T-C

104095561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6231135-A-G

104095804-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6230913-G-C

104096027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6229958-A-G

104096048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6229939-A-G

104096179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6229811-T-C

104105000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6229285-A-G

104105112-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6229178-T-A

104105162-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6229131-T-G

104105245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6229049-G-T

104105878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6228450-T-C

http://identifiers.org/hco/11/GRCh38#104106042-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6228223-A-C

104106201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6228057-T-C

104106586-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6224829-G-C

104106587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6224828-G-A

104106852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6224635-G-T

104106887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6224601-G-T

104107057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6224526-T-C

104107057-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6224526-T-G

104107073-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6224511-T-A

104107198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6224390-G-A

http://identifiers.org/hco/11/GRCh38#104121066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6219780-C-A

104123341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6217816-T-C

http://identifiers.org/hco/11/GRCh38#104123383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6217774-C-A

104123383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6217774-C-T

104123557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6217603-T-C

104123564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6217596-C-T

104123779-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6217385-T-G

104124113-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6217081-T-A

104124113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6217081-T-C

104124165-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6217030-G-C

104124608-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6216418-G-C

104124713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6216332-C-T

http://identifiers.org/hco/11/GRCh38#104124982-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6216086-A-C

104128751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6215886-A-G

104128797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6215841-T-C

104128971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6215684-C-T

104129056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6215623-T-C

104130016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6214703-G-A

104130016-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6214703-G-C

104130016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6214703-G-T

104130064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6214651-G-A

104130123-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6214588-C-G

104130364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6214406-G-A

http://identifiers.org/hco/11/GRCh38#104130379-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6214391-A-C

104130379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6214391-A-G

104131077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6213340-T-C

104131108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6213311-A-G

104131234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6213188-T-C

104131316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6213083-T-C

104131421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6212977-G-A

http://identifiers.org/hco/11/GRCh38#104131531-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6212877-A-C

104131565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6212844-T-C

104131596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6212815-G-T

104131632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6212781-C-T

http://identifiers.org/hco/11/GRCh38#104131761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6212631-C-A

104131761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6212631-C-T

104131862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6212553-G-A

104131956-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6212459-C-G

104132015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6212264-C-T

104132066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6212218-T-C

http://identifiers.org/hco/11/GRCh38#104132082-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6212203-A-C

104132084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6212201-T-C

http://identifiers.org/hco/11/GRCh38#104132212-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6212073-A-C

104132261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6212015-G-A

104132895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6211119-G-A

104133018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6210966-T-C

104133275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6209776-A-G

104133302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6209749-A-G

104133375-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6209668-T-G

104133436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6209610-C-T

104133779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6209296-T-C

104133976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6209121-G-A

http://identifiers.org/hco/11/GRCh38#104134160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6208929-C-A

104134171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6208920-G-A

104134171-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6208920-G-C

104134222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6208873-T-C

104134715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6208344-G-A

104135424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6206736-G-A

104135618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6206541-A-G

104135827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6206380-T-C

104135844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6206362-T-C

104135862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6206344-T-C

104135965-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6206248-G-C

104135965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6206248-G-T

104136325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6205938-T-C

104137183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6199333-T-C

104137231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6199289-G-T

104137579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6198171-T-C

104137786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6197977-C-T

104137811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6197956-G-A

104137912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6197821-T-C

http://identifiers.org/hco/11/GRCh38#104138024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6197700-C-A

104138468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6197288-T-C

104138734-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6197012-C-G

104138734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6197012-C-T

104138768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6196981-C-T

104139193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6196771-C-T

104139328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6196672-G-A

104139407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6196596-G-A

http://identifiers.org/hco/11/GRCh38#104139631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6196432-C-A

104139711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6196360-G-A

104140114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6196308-G-A

104140207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6196211-T-C

104140266-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6196153-G-C

104140397-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6196025-T-G

104140460-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6195986-T-A

104140463-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6195983-G-C

104140644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6195812-A-G

104140971-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6195462-C-G

104141011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6195400-C-T

104144829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6193681-C-T

104145124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6193282-G-A

104145309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6193109-T-C

104145689-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6189502-C-G

104146172-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6189024-A-T

104146364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6188873-G-A

104146371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6188866-G-T

104146670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6188560-T-C

104147117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6188167-T-C

104147141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6188152-A-G

104147352-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6187986-C-G

104147364-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6187974-T-G

104147934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6187433-T-C

104148060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6187343-T-C

104148060-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6187343-T-G

104148268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron_variant, undefined
orthologous variants: 6187117-A-G

104148574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6186816-A-G

http://identifiers.org/hco/11/GRCh38#104150943-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6186033-A-C

104150980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6186006-T-C

104151020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6185959-G-A

104151081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6185903-C-T

104151102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6185883-T-C

104151246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6185678-G-A

http://identifiers.org/hco/11/GRCh38#104151412-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6185445-A-C

104151467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6185389-A-G

104151557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6185278-T-C

104151557-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6185278-T-G

104151798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6185019-T-C

104151839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6184986-T-C

104151960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6184851-G-A

104153605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6181904-A-G

104153726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6181800-T-C

104153749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6181777-T-C

http://identifiers.org/hco/11/GRCh38#104153796-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6181721-A-C

104153952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6181580-G-A

http://identifiers.org/hco/11/GRCh38#104154342-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6181163-A-C

104154553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6180966-T-C

104154638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6180874-T-C

104154697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6180816-G-A

104154735-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6180773-A-T

http://identifiers.org/hco/11/GRCh38#104154743-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6180765-A-C

104154767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6180741-A-G

104155477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6178622-T-C

104155477-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6178622-T-G

104155491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6178607-C-T

104155506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6178592-G-A

104155630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6178461-G-T

104155633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6178458-T-C

104155807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6178290-A-G

104155807-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6178290-A-T

104155999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6178131-C-T

104156105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6178032-T-C

104156440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6177841-T-C

104156592-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6177697-T-G

104156625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6177667-C-T

104156655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6177651-T-C

104156698-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6177609-G-C

104156868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6177462-T-C

http://identifiers.org/hco/11/GRCh38#104157180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6177174-C-A

104157180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6177174-C-T

104157198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6177158-G-A

104157206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6177150-G-A

104157332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6177022-C-T

104159232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6175620-C-T

104159268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6175591-C-T

http://identifiers.org/hco/11/GRCh38#104159293-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6175566-A-C

104159537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6175380-A-G

104159668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6175278-T-C

104159738-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6175209-T-G

104159863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6173773-G-A

104160263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6173349-A-G

104160314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6173308-G-A

104160539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6173137-G-A

104160838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6172879-G-A

http://identifiers.org/hco/11/GRCh38#104161147-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6172384-A-C

104161263-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6172293-T-A

http://identifiers.org/hco/11/GRCh38#104161280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6172276-C-A

104161409-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6172144-T-G

104161472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6172089-C-T

104161557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6171897-A-G

http://identifiers.org/hco/11/GRCh38#104161574-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6171867-A-C

104161587-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6171854-T-A

http://identifiers.org/hco/11/GRCh38#104161626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6171815-C-A

http://identifiers.org/hco/11/GRCh38#104161642-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6171799-C-A

104161650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6171791-A-G

104161659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6171779-C-T

http://identifiers.org/hco/11/GRCh38#104161674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6171764-C-A

104161674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6171764-C-T

http://identifiers.org/hco/11/GRCh38#104161679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6171759-C-A

104161679-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6171759-C-G

104161679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6171759-C-T

104161844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6171664-T-C

104161950-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6171563-A-T

104161954-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6171559-T-A

104161961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6171552-G-A

104161966-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6171547-T-A

104161977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6171536-G-A

104162035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6171485-C-T

104162171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6171356-G-A

104162572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6170153-T-C

104162643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6170084-C-T

104162812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6169934-G-A

104162828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6169901-T-C

104162934-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6169781-C-G

104162934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6169781-C-T

104162988-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6169731-G-C

104162988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6169731-G-T

104162999-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6169720-C-G

104163007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6169712-A-G

104163395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6169361-A-G

104163481-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6169301-T-G

104163521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6169262-G-A

104163635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6169144-T-C

104163665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6169062-G-T

http://identifiers.org/hco/11/GRCh38#104163676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6169053-C-A

104163676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6169053-C-T

104163748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6168974-A-G

104163774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: intron variant
orthologous variants: 6168946-T-C

104163845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: missense variant
orthologous variants: 6168875-G-A

104163870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: missense variant
orthologous variants: 6168850-C-T

104163895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: synonymous variant
orthologous variants: 6168825-G-A

104163895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: synonymous variant
orthologous variants: 6168825-G-T

104163931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 5 prime UTR variant
orthologous variants: 6168789-G-A

104163931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 5 prime UTR variant
orthologous variants: 6168789-G-T

104163937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 5 prime UTR variant
orthologous variants: 6168783-G-A

104163937-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 5 prime UTR variant
orthologous variants: 6168783-G-C

104163946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 5 prime UTR variant
orthologous variants: 6168773-G-A

104163946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 5 prime UTR variant
orthologous variants: 6168773-G-T

104163947-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 5 prime UTR variant
orthologous variants: 6168772-A-T

104163962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 5 prime UTR variant
orthologous variants: 6168757-G-A

104163962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 5 prime UTR variant
orthologous variants: 6168757-G-T

http://identifiers.org/hco/11/GRCh38#104163983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6168724-C-A

104163983-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 5 prime UTR variant
orthologous variants: 6168724-C-G

104163983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 5 prime UTR variant
orthologous variants: 6168724-C-T

104163985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 5 prime UTR variant
orthologous variants: 6168722-G-T

104164014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 5 prime UTR variant
orthologous variants: 6168693-G-A

104164014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 5 prime UTR variant
orthologous variants: 6168693-G-T

104164020-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 6168687-T-A

104164020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 6168687-T-C

http://identifiers.org/hco/11/GRCh38#104164040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6168679-C-A

104164040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 5 prime UTR variant
orthologous variants: 6168679-C-T

http://identifiers.org/hco/11/GRCh38#104164061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#6168658-C-A

104164061-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 5 prime UTR variant
orthologous variants: 6168658-C-G

104164061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 5 prime UTR variant
orthologous variants: 6168658-C-T

http://identifiers.org/hco/11/GRCh38#104164116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#6168603-C-A

104164152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 6168567-G-A

104164152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 6168567-G-T

104164198-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 6168524-C-G

104164198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 6168524-C-T

104164199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 6168523-G-A

104164199-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 6168523-G-C

104164199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 6168523-G-T

104164232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 5 prime UTR variant
orthologous variants: 6168490-G-A

104164232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 5 prime UTR variant
orthologous variants: 6168490-G-T

104164372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 6168386-G-T

104164373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30620
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 6168385-C-T